NUCLEOTIDE-SEQUENCE AND EXPRESSION OF A CDNA-ENCODING CHICK BRAIN ACTIN DEPOLYMERIZING FACTOR

被引:57
作者
ADAMS, ME [1 ]
MINAMIDE, LS [1 ]
DUESTER, G [1 ]
BAMBURG, JR [1 ]
机构
[1] COLORADO STATE UNIV,DEPT BIOCHEM,FT COLLINS,CO 80523
关键词
D O I
10.1021/bi00484a009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chick brain actin depolymerizing factor (ADF) is a 19-kDa protein that severs actin filaments and binds actin monomers. We have obtained a cDNA encoding ADF by screening a chick embryo λgt11 cDNA library with both a rabbit anti-ADF antiserum and two oligonucleotide probes. Several non-full-length clones of 636 bases and one full-length clone of 1886 bases were isolated and sequenced. The full-length cDNA encodes a protein of 165 amino acids with a calculated molecular weight of 18 520. The deduced amino acid sequence shows 73% identity with the porcine brain actin binding protein cofilin. The coding region of the ADF cDNA has been placed in an expression vector, and the resulting protein shows immunoreactivity with an anti-ADF antiserum but not with an anti-cofilin antibody. The expressed ADF has been purified and has an actin depolymerizing activity identical with that of brain ADF. Like cofilin, ADF contains a sequence similar to the nuclear transport signal sequence of the SV40 large T antigen and a calcium/calmodulin-dependent protein kinase II phosphorylation consensus sequence. Northern blots of both embryonic chick brain and muscle RNA revealed two ADF mRNAs of length 2.1 and 0.9 kilobases. Southern blots suggest that the ADF gene is present in a single copy within the chicken genome. ADF contains regions of homology with other actin binding proteins including tropomyosin, gelsolin, and depactin. © 1990, American Chemical Society. All rights reserved.
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页码:7414 / 7420
页数:7
相关论文
共 40 条
[1]   A COFILIN-LIKE PROTEIN IS INVOLVED IN THE REGULATION OF ACTIN ASSEMBLY IN DEVELOPING SKELETAL-MUSCLE [J].
ABE, H ;
OHSHIMA, S ;
OBINATA, T .
JOURNAL OF BIOCHEMISTRY, 1989, 106 (04) :696-702
[2]  
ABE H, 1990, BIOCHEM, V29, P7425
[3]  
ABE H, 1989, CELLULAR MOL BIOL MU, P197
[4]   PARTIAL-PURIFICATION AND CHARACTERIZATION OF AN ACTIN DEPOLYMERIZING FACTOR FROM BRAIN [J].
BAMBURG, JR ;
HARRIS, HE ;
WEEDS, AG .
FEBS LETTERS, 1980, 121 (01) :178-182
[5]   DISTRIBUTION AND CELLULAR-LOCALIZATION OF ACTIN DEPOLYMERIZING FACTOR [J].
BAMBURG, JR ;
BRAY, D .
JOURNAL OF CELL BIOLOGY, 1987, 105 (06) :2817-2825
[6]   PROTEIN-KINASES 1988 - A CURRENT PERSPECTIVE [J].
BLACKSHEAR, PJ ;
NAIRN, AC ;
KUO, JF .
FASEB JOURNAL, 1988, 2 (14) :2957-2969
[7]   SELECTIVE ASSAY OF MONOMERIC AND FILAMENTOUS ACTIN IN CELL-EXTRACTS, USING INHIBITION OF DEOXYRIBONUCLEASE-I [J].
BLIKSTAD, I ;
MARKEY, F ;
CARLSSON, L ;
PERSSON, T ;
LINDBERG, U .
CELL, 1978, 15 (03) :935-943
[8]  
CHIRGWIN JM, 1979, BIOCHEMISTRY-US, V18, P5295
[9]  
CHO YJ, 1990, J BIOL CHEM, V265, P538
[10]   AMINO-ACID-SEQUENCES SURROUNDING THE CAMP-DEPENDENT AND CALCIUM CALMODULIN-DEPENDENT PHOSPHORYLATION SITES IN RAT AND BOVINE SYNAPSIN-I [J].
CZERNIK, AJ ;
PANG, DT ;
GREENGARD, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7518-7522